EURICAN DAP LYOPHILISATE AND SOLVENT FOR SUSPENSION FOR INJECTION
EURICAN DAP LYOPHILISATE AND SOLVENT FOR SUSPENSION FOR INJECTION
Authorised
This information is not available for this product.
Product identification
Medicine name:
EURICAN DAP LYOPHILISATE AND SOLVENT FOR SUSPENSION FOR INJECTION
Eurican DAP λυοφιλοποιημένο υλικό και διαλύτης για ενέσιμο εναιώρημα
Active substance:
This information is not available for this product.
Target species:
-
Dog
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
This information is not available for this product.
Pharmaceutical form:
-
Lyophilisate and solvent for suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI07AD02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Cyprus
Package description:
- Plastic box of 10 vials of lyophilisate (1 dose) and 10 vials of solvent (1 ml)
- Plastic box of 50 vials of lyophilisate (1 dose) and 50 vials of solvent (1 ml)
- Plastic box of 10 vials of lyophilisate (1 dose)
- Plastic box of 50 vials of lyophilisate (1 dose)
- Plastic box of 10 vials of solvent (1 ml)
- Plastic box of 50 vials of solvent (1 ml)
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Boehringer Ingelheim Animal Health France
Marketing authorisation date:
Manufacturing sites for batch release:
- Boehringer Ingelheim Animal Health France
Responsible authority:
- Veterinary Services, Ministry Of Agriculture, Natural Resources And Environment
Authorisation number:
- CY00562V
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0305/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Malta
-
Netherlands
-
Norway
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
How useful was this page?: